rs587779267
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing.
|
26681312 |
2016 |
rs587782712
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Lynch syndrome mutation spectrum in New South Wales, Australia, including 55 novel mutations.
|
27064304 |
2016 |
rs63749942
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Germline multi-gene hereditary cancer panel testing in an unselected endometrial cancer cohort.
|
27443514 |
2016 |
rs63750111
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Mismatch repair gene mutation spectrum in the Swedish Lynch syndrome population.
|
27601186 |
2016 |
rs63750767
|
|
TTCAAAAGGGACATAGAAAA |
0.700 |
CausalMutation |
CLINVAR |
A cohort analysis of men with a family history of BRCA1/2 and Lynch mutations for prostate cancer.
|
27456091 |
2016 |
rs63750767
|
|
TTCAAAAGGGACATAGAAAA |
0.700 |
CausalMutation |
CLINVAR |
Improving performance of multigene panels for genomic analysis of cancer predisposition.
|
26845104 |
2016 |
rs63750767
|
|
TTCAAAAGGGACATAGAAAA |
0.700 |
CausalMutation |
CLINVAR |
Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing.
|
26681312 |
2016 |
rs730881816
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing.
|
26681312 |
2016 |
rs730881827
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing.
|
26681312 |
2016 |
rs730881830
|
|
TTC |
0.700 |
CausalMutation |
CLINVAR |
Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing.
|
26681312 |
2016 |
rs760190301
|
|
AAGTT |
0.700 |
CausalMutation |
CLINVAR |
Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing.
|
26681312 |
2016 |
rs863225421
|
|
CG |
0.700 |
CausalMutation |
CLINVAR |
Mismatch repair gene mutation spectrum in the Swedish Lynch syndrome population.
|
27601186 |
2016 |
rs864622153
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Mismatch repair gene mutation spectrum in the Swedish Lynch syndrome population.
|
27601186 |
2016 |
rs1060502886
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Prognostic impact of mismatch repair genes germline defects in colorectal cancer patients: are all mutations equal?
|
26485756 |
2015 |
rs1060502888
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Lynch-like syndrome: characterization and comparison with EPCAM deletion carriers.
|
25110875 |
2015 |
rs1060502926
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Multigene panel analysis identified germline mutations of DNA repair genes in breast and ovarian cancer.
|
26436112 |
2015 |
rs146816935
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Combined Microsatellite Instability, MLH1 Methylation Analysis, and Immunohistochemistry for Lynch Syndrome Screening in Endometrial Cancers From GOG210: An NRG Oncology and Gynecologic Oncology Group Study.
|
26552419 |
2015 |
rs1553333175
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
[Constitutional mismatch repair deficiency syndrome].
|
26200421 |
2015 |
rs267608042
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Clinical characterization and mutation spectrum in Caribbean Hispanic families with Lynch syndrome.
|
25782445 |
2015 |
rs267608077
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Impact of an immunohistochemistry-based universal screening protocol for Lynch syndrome in endometrial cancer on genetic counseling and testing.
|
25617771 |
2015 |
rs267608078
|
|
AC |
0.700 |
CausalMutation |
CLINVAR |
Constitutional mismatch repair deficiency syndrome: clinical description in a French cohort.
|
26318770 |
2015 |
rs267608094
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Constitutional mismatch repair deficiency syndrome: clinical description in a French cohort.
|
26318770 |
2015 |
rs267608098
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Identification of a Variety of Mutations in Cancer Predisposition Genes in Patients With Suspected Lynch Syndrome.
|
25980754 |
2015 |
rs267608120
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Genetic features of Lynch syndrome in the Israeli population.
|
25430799 |
2015 |
rs267608121
|
|
ATCAG |
0.700 |
CausalMutation |
CLINVAR |
Identification of germline genetic mutations in patients with pancreatic cancer.
|
26440929 |
2015 |